| Literature DB >> 26860321 |
Mahmoud Labib1, Brenda Green2, Reza M Mohamadi1, Adam Mepham2, Sharif U Ahmed1, Laili Mahmoudian1, I-Hsin Chang1, Edward H Sargent, Shana O Kelley1,2.
Abstract
Cancer cells, and in particular those found circulating in blood, can have widely varying phenotypes and molecular profiles despite a common origin. New methods are needed that can deconvolute the heterogeneity of cancer cells and sort small numbers of cells to aid in the characterization of cancer cell subpopulations. Here, we describe a new molecular approach to capturing cancer cells that isolates subpopulations using two-dimensional sorting. Using aptamer-mediated capture and antisense-triggered release, the new strategy sorts cells according to levels of two different markers and thereby separates them into their corresponding subpopulations. Using a phenotypic assay, we demonstrate that the subpopulations isolated have markedly different properties. This system provides an important new tool for identifying circulating tumor cell subtypes.Entities:
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Year: 2016 PMID: 26860321 DOI: 10.1021/jacs.5b10939
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419